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Structural Insights into De Novo Promoter Escape by Mycobacterium tuberculosis RNA Polymerase
by
Zoullas, Winston Bates
, Brewer, Joshua
, Darst, Seth A.
, Delbeau, Madeleine
, Campbell, Elizabeth A.
in
631/337/2265
/ 631/337/572
/ 631/535/1258/1259
/ Antibiotics
/ Bacteria
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biochemistry
/ Cryoelectron Microscopy
/ DNA, Bacterial - genetics
/ DNA, Bacterial - metabolism
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - chemistry
/ DNA-Directed RNA Polymerases - genetics
/ DNA-Directed RNA Polymerases - metabolism
/ DNA-Directed RNA Polymerases - ultrastructure
/ Electron microscopy
/ Enzymes
/ Gene expression
/ Humanities and Social Sciences
/ Intermediates
/ Models, Molecular
/ multidisciplinary
/ Mycobacterium tuberculosis - enzymology
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Promoter Regions, Genetic - genetics
/ Ribonucleic acid
/ Rifampin
/ Rifampin - pharmacology
/ RNA
/ RNA polymerase
/ Science
/ Science (multidisciplinary)
/ Sigma Factor - metabolism
/ Transcription initiation
/ Transcription, Genetic
/ Tuberculosis
2025
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Structural Insights into De Novo Promoter Escape by Mycobacterium tuberculosis RNA Polymerase
by
Zoullas, Winston Bates
, Brewer, Joshua
, Darst, Seth A.
, Delbeau, Madeleine
, Campbell, Elizabeth A.
in
631/337/2265
/ 631/337/572
/ 631/535/1258/1259
/ Antibiotics
/ Bacteria
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biochemistry
/ Cryoelectron Microscopy
/ DNA, Bacterial - genetics
/ DNA, Bacterial - metabolism
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - chemistry
/ DNA-Directed RNA Polymerases - genetics
/ DNA-Directed RNA Polymerases - metabolism
/ DNA-Directed RNA Polymerases - ultrastructure
/ Electron microscopy
/ Enzymes
/ Gene expression
/ Humanities and Social Sciences
/ Intermediates
/ Models, Molecular
/ multidisciplinary
/ Mycobacterium tuberculosis - enzymology
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Promoter Regions, Genetic - genetics
/ Ribonucleic acid
/ Rifampin
/ Rifampin - pharmacology
/ RNA
/ RNA polymerase
/ Science
/ Science (multidisciplinary)
/ Sigma Factor - metabolism
/ Transcription initiation
/ Transcription, Genetic
/ Tuberculosis
2025
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Structural Insights into De Novo Promoter Escape by Mycobacterium tuberculosis RNA Polymerase
by
Zoullas, Winston Bates
, Brewer, Joshua
, Darst, Seth A.
, Delbeau, Madeleine
, Campbell, Elizabeth A.
in
631/337/2265
/ 631/337/572
/ 631/535/1258/1259
/ Antibiotics
/ Bacteria
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biochemistry
/ Cryoelectron Microscopy
/ DNA, Bacterial - genetics
/ DNA, Bacterial - metabolism
/ DNA-directed RNA polymerase
/ DNA-Directed RNA Polymerases - chemistry
/ DNA-Directed RNA Polymerases - genetics
/ DNA-Directed RNA Polymerases - metabolism
/ DNA-Directed RNA Polymerases - ultrastructure
/ Electron microscopy
/ Enzymes
/ Gene expression
/ Humanities and Social Sciences
/ Intermediates
/ Models, Molecular
/ multidisciplinary
/ Mycobacterium tuberculosis - enzymology
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Promoter Regions, Genetic - genetics
/ Ribonucleic acid
/ Rifampin
/ Rifampin - pharmacology
/ RNA
/ RNA polymerase
/ Science
/ Science (multidisciplinary)
/ Sigma Factor - metabolism
/ Transcription initiation
/ Transcription, Genetic
/ Tuberculosis
2025
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Structural Insights into De Novo Promoter Escape by Mycobacterium tuberculosis RNA Polymerase
Journal Article
Structural Insights into De Novo Promoter Escape by Mycobacterium tuberculosis RNA Polymerase
2025
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Overview
Transcription in bacteria is a multi-step process. In the first step, contacts between RNA polymerase and the promoter DNA must be established for transcription initiation to begin, but then these contacts must be broken for the enzyme to transition into the elongation phase. Single-molecule and biochemical observations report that promoter escape is a highly regulated and sometimes rate-limiting step in the transcription cycle; however, the structural mechanisms of promoter escape remain obscure. Promoter escape also serves as the target for the clinically important antibiotic rifampicin, used to treat tuberculosis. Here, we present seven distinct intermediates showing the structural details of
M. tuberculosis
RNA polymerase initial transcribing complexes and promoter escape, using a de novo cryo-electron microscopy approach. We describe the structural rearrangements that RNA polymerase undergoes to clear the promoter, including those required to release the initiation factor, σ, providing a structural account for decades of biochemical observations. These structures and supporting biochemistry provide a model of promoter escape, a universal step in the transcription cycle, with conformations that may be used to develop Rifampicin alternatives.
Promoter escape is a key step in bacterial transcription and a target of the antibiotic rifampicin. Here, the authors use cryo-EM to explore this step, finding seven structural intermediates of
M. tuberculosis
RNA polymerase during promoter escape.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Bacteria
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ DNA-Directed RNA Polymerases - chemistry
/ DNA-Directed RNA Polymerases - genetics
/ DNA-Directed RNA Polymerases - metabolism
/ DNA-Directed RNA Polymerases - ultrastructure
/ Enzymes
/ Humanities and Social Sciences
/ Mycobacterium tuberculosis - enzymology
/ Mycobacterium tuberculosis - genetics
/ Mycobacterium tuberculosis - metabolism
/ Promoter Regions, Genetic - genetics
/ Rifampin
/ RNA
/ Science
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